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A systems immunology study comparing innate and adaptive immune responses in adults to COVID-19 mRNA and adenovirus vectored vaccines.

Feargal J Ryan | Todd S Norton | Conor McCafferty | Stephen J Blake | Natalie E Stevens | Jane James | Georgina L Eden | Yee C Tee | Saoirse C Benson | Makutiro G Masavuli | Arthur E L Yeow | Arunasingam Abayasingam | David Agapiou | Hannah Stevens | Jana Zecha | Nicole L Messina | Nigel Curtis | Vera Ignjatovic | Paul Monagle | Huyen Tran | James D McFadyen | Rowena A Bull | Branka Grubor-Bauk | Miriam A Lynn | Rochelle Botten | Simone E Barry | David J Lynn
Cell reports. Medicine | 2023

Identifying the molecular mechanisms that promote optimal immune responses to coronavirus disease 2019 (COVID-19) vaccination is critical for future rational vaccine design. Here, we longitudinally profile innate and adaptive immune responses in 102 adults after the first, second, and third doses of mRNA or adenovirus-vectored COVID-19 vaccines. Using a multi-omics approach, we identify key differences in the immune responses induced by ChAdOx1-S and BNT162b2 that correlate with antigen-specific antibody and T cell responses or vaccine reactogenicity. Unexpectedly, we observe that vaccination with ChAdOx1-S, but not BNT162b2, induces an adenoviral vector-specific memory response after the first dose, which correlates with the expression of proteins with roles in thrombosis with potential implications for thrombosis with thrombocytopenia syndrome (TTS), a rare but serious adverse event linked to adenovirus-vectored vaccines. The COVID-19 Vaccine Immune Responses Study thus represents a major resource that can be used to understand the immunogenicity and reactogenicity of these COVID-19 vaccines.

Pubmed ID: 36871558 RIS Download

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Hu CCR7 (CD197) BV421 2-L1-A (antibody)

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APC anti-human CD137 (4-1BB) (antibody)

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CD123 (IL-3 Receptor α) (antibody)

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FITC anti-human CD45RA (antibody)

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Hu CD45 BUV395 HI30 100Tst (antibody)

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CD38 (antibody)

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